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| Status |
Public on Jan 16, 2013 |
| Title |
aCGH was used to identify the overall genomic imbalances of SCC of the vulva in 14 patients |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
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| Summary |
The imbalances scored by arrayCGH mapped to different chromosomes with losses being more common than gains. Frequent losses of large chromosomal segments were scored from 3p and 8p whereas same-sized gains were frequent from 3q and 8q. This is the first study of vulvar tumors using arrayCGH, and some frequent imbalances could be defined precisely.
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| Overall design |
14 patients we analyzed without replicates against a commercial common reference.
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| Contributor(s) |
Micci F, Heim S |
| Citation(s) |
23404381 |
| |
| Submission date |
May 24, 2012 |
| Last update date |
Apr 17, 2013 |
| Contact name |
Francesca Micci |
| E-mail(s) |
francesca.micci@medisin.uio.no
|
| Organization name |
Oslo Universitetssykehus
|
| Department |
Institute for medical informatics
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| Lab |
cancer cytogenetics
|
| Street address |
Ullernchausseen 70
|
| City |
oslo |
| ZIP/Postal code |
0310 |
| Country |
Norway |
| |
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| Platforms (1) |
| GPL10123 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version) |
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| Samples (14)
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| This SubSeries is part of SuperSeries: |
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| Relations |
| BioProject |
PRJNA167468 |
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